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    <titleInfo>
      <title>PENGEMBANGAN VAKSIN KOLERA UNGGAS</title>
      <subTitle>I. PROTEKSI VAKSIN  PASTEURELLA MULTOCIDA ISOLAT LOKAL PADA AYAM  TERHADAP UJI TANTANG GALUR HOMOLOG DAN HETEROLOG</subTitle>
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    <name type="personal" usage="primary">
      <namePart>SUPAR</namePart>
    </name>
    <typeOfResource>text</typeOfResource>
    <originInfo>
      <place>
        <placeTerm type="text">Balai Penelitian Veteriner</placeTerm>
      </place>
      <publisher>Jurnal Ilmu Ternak dan Veteriner</publisher>
      <dateIssued>2001</dateIssued>
      <edition>Vol. 6 No. 1</edition>
      <issuance/>
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      <extent>9</extent>
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    <abstract type="Summary">Pasteurella multocida locally isolated from chicken and ducks (BCC 299, BCC 2331, DY1, DY2, 12TG, 15TG) and &#13;
imported strains (BCC 1359, 1362; HEDDLESTON group 1 and 6 respectively) had been tested for its pathogenicity in the &#13;
previous study. The aims of this experiment were to study the preparation of local isolate pasteurellosis vaccines and to &#13;
determine the protective effect of that vaccines in chicken against the highly pathogenic local isolates of P. multocida. Killed &#13;
monovalent, bivalent and polyvalent pasteurellosis vaccines were prepared and each was adjunvanted with aluminum hydroxide &#13;
gel at a final concentration of 1.5% and the cell concentration was equal to the No 10 of MacFarland tube standard. Each of the &#13;
vaccine prepared was used to vaccinated on a group of six week old of layer chicken (8 per group). Each chicken was &#13;
subcutaneously injected with 0.2 ml of vaccine, four weeks later each was boostered with similar vaccine with the same dose. &#13;
Two weeks after giving the boostered vaccine each group of chicken were challenged, half with life bacterium of P. multocida &#13;
BCC 2331 and other with DY2. Any chick which survive after challenge was designated as protected by vaccination. Before &#13;
vaccination 1 ml of blood was drawn from each of chicken and then two weeks apart up to challenge. Serum from each sample &#13;
was separated and kept in deep freeze until tested by enzyme-linked immunosorbent assay (ELISA). Chicken vaccinated with &#13;
killed whole cell P. multocida vaccines of monovalent (BCC 2331 or DY2) and bivalent (BCC 2331 + DY2) were protected &#13;
against challenge with live bacterium of either BCC 2331 or DY2 at rate 67-100%. There was no protection in chicken &#13;
vaccinated with either BCC 299, DY1, 12TG, 15TG, BCC 1359, or 1362 killed vaccine. Similarly no protection of chicken &#13;
vaccinated with either DY1 + BCC299, 12TG + 15TG or BCC 1359 + BCC 1362 bivalent vaccines. The protection rate of the &#13;
polyvalent local isolate vaccine was at average 50-75%. All vaccinated chicken showed the presence of antibody responses &#13;
againsted the extract cell and whole cell antigens of either P. multocida BCC 2331 or DY2 local isolate as detected by ELISA. &#13;
The antibody responses from vaccinated chicken against extra cellular antigens prepared from broth cultures of BCC 2331 and &#13;
DY2 were detected only from vaccinated chicken with vaccine containing killed antigen of BCC 2331 and/or DY2 isolate. It is &#13;
likely, the local isolate of P. multocida BCC 2331 and DY2 would be benefit for producing inactive fowl cholera vaccine use in &#13;
Indonesia, but the protective antigen that enhances immune protection should be determined by means of immunoblotting &#13;
techniques. &#13;
Key words: Pasteurella multocida, fowl cholera, vaccine, protection</abstract>
    <note type="statement of responsibility" altRepGroup="00">SUPAR</note>
    <subject>
      <topic>VAKSIN KOLERA</topic>
    </subject>
    <classification authority="ddc">ARTVET0592</classification>
    <classification authority="">ARTVET0592</classification>
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      <recordCreationDate encoding="marc">250109</recordCreationDate>
      <recordChangeDate encoding="iso8601">20250109081657</recordChangeDate>
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